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Coupling constants in N-substituted pyridines and their relation with electronegativity

✍ Scribed by Alan R. Katritzky; Michael Kinns; Edward Lunt


Book ID
102531277
Publisher
John Wiley and Sons
Year
1975
Tongue
English
Weight
205 KB
Volume
7
Category
Article
ISSN
0749-1581

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✦ Synopsis


Abstract

The coupling constants obtained from the complete spectral analysis of series of 1‐ and 3‐substituted pyridine N‐imides are related linearly to the electronegativities of the substituent atoms. The main conclusions of the papers by Cox, Castellano and Sun, and Castellano and Kostelnik are substantiated. The inductive effects of the first atoms of the substituents largely determine the coupling between protons in the ring system; delocalisation of π‐electrons in the ring produces a much smaller effect.


πŸ“œ SIMILAR VOLUMES


15N,1H coupling constants in pyridines a
✍ W. StΓ€deli; P. Bigler; W. Von Philipsborn πŸ“‚ Article πŸ“… 1981 πŸ› John Wiley and Sons 🌐 English βš– 282 KB

## Abstract Application of a modified INEPT pulse sequence to obtain fully proton‐coupled and selectively decoupled ^15^N NMR spectra of pyridines and pyrimidines with natural isotope abundance is demonstrated. The spectra are analysed for ^2^__J__, ^3^__J__ and ^4^J(NH) coupling constants.